UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.73219229C= , CM000676.2:g.73219229C= | GRCh38 |
| NC_000014.8:g.73685937C= , CM000676.1:g.73685937C= | GRCh37 |
| NC_000014.7:g.72755690C= | NCBI36 |
| NG_007386.2:g.87759C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000553599.6:c.1332C= | ENSP00000452477.2:p.Ala444= | |
| ENST00000554131.6:c.1344C= | ENSP00000451915.2:p.Ala448= | |
| ENST00000554995.2:n.2094C= | ||
| ENST00000555386.6:c.*299C= | ENSP00000450845.1:n.*299C= | |
| ENST00000556066.2:n.1770C= | ||
| ENST00000556951.6:c.1332C= | ENSP00000450551.2:p.Ala444= | |
| ENST00000557293.6:c.1224C= | ENSP00000451880.2:p.Ala408= | |
| ENST00000559361.6:c.*1288C= | ENSP00000454156.1:n.*1288C= | |
| ENST00000697912.1:c.*532C= | ENSP00000513477.1:n.*532C= | |
| ENST00000697913.1:n.6894C= | ||
| ENST00000697915.1:n.701C= | ||
| ENST00000700265.1:c.1332C= | ENSP00000514901.1:p.Ala444= | |
| ENST00000700266.1:c.*1556C= | ENSP00000514902.1:n.*1556C= | |
| ENST00000700267.1:c.1344C= | ENSP00000514903.1:p.Ala448= | |
| ENST00000700268.1:c.1344C= | ENSP00000514904.1:p.Ala448= | |
| ENST00000700269.1:c.1344C= | ENSP00000514905.1:p.Ala448= | |
| ENST00000700271.1:c.1158C= | ENSP00000514906.1:p.Ala386= | |
| ENST00000700272.1:c.*1288C= | ENSP00000514907.1:n.*1288C= | |
| ENST00000700273.1:c.1332C= | ENSP00000514908.1:p.Ala444= | |
| ENST00000700302.1:c.*160C= | ENSP00000514929.1:n.*160C= | |
| ENST00000700303.1:c.*1006C= | ENSP00000514930.1:n.*1006C= | |
| ENST00000700304.1:c.*1288C= | ENSP00000514931.1:n.*1288C= | |
| ENST00000700305.1:c.*902C= | ENSP00000514932.1:n.*902C= | |
| ENST00000700306.1:c.1344C= | ENSP00000514933.1:p.Ala448= | |
| ENST00000700307.1:c.1245C= | ENSP00000514934.1:p.Ala415= | |
| ENST00000700308.1:c.*1288C= | ENSP00000514935.1:n.*1288C= | |
| ENST00000700309.1:c.*1433C= | ENSP00000514936.1:n.*1433C= | |
| ENST00000700310.1:c.*299C= | ENSP00000514937.1:n.*299C= | |
| ENST00000700311.1:c.*160C= | ENSP00000514938.1:n.*160C= | |
| ENST00000700312.1:c.1095C= | ENSP00000514939.1:p.Ala365= | |
| ENST00000700313.1:c.1332C= | ENSP00000514940.1:p.Ala444= | |
| ENST00000700314.1:c.*1283C= | ENSP00000514941.1:n.*1283C= | |
| ENST00000700315.1:c.*902C= | ENSP00000514942.1:n.*902C= | |
| ENST00000700316.1:c.*1124C= | ENSP00000514943.1:n.*1124C= | |
| ENST00000700317.1:c.1344C= | ENSP00000514944.1:p.Ala448= | |
| ENST00000700318.1:c.*1006C= | ENSP00000514945.1:n.*1006C= | |
| ENST00000700319.1:c.*784C= | ENSP00000514946.1:n.*784C= | |
| ENST00000700320.1:c.1371C= | ENSP00000514947.1:p.Ala457= | |
| ENST00000700321.1:c.1344C= | ENSP00000514948.1:p.Ala448= | |
| ENST00000700322.1:c.1332C= | ENSP00000514949.1:p.Ala444= | |
| ENST00000700323.1:c.1344C= | ENSP00000514950.1:p.Ala448= | |
| ENST00000700324.1:c.1332C= | ENSP00000514951.1:p.Ala444= | |
| ENST00000700375.1:c.1344C= | ENSP00000514966.1:p.Ala448= | |
| ENST00000700377.1:c.*812C= | ENSP00000514967.1:n.*812C= | |
| ENST00000700378.1:c.1344C= | ENSP00000514968.1:p.Ala448= | |
| ENST00000700379.1:n.1742C= | ||
| ENST00000700389.1:c.1332C= | ENSP00000514970.1:p.Ala444= | |
| ENST00000700390.1:n.3055C= | ||
| ENST00000700391.1:n.555C= | ||
| ENST00000700404.1:n.2343C= | ||
| ENST00000700436.1:c.*299C= | ENSP00000514987.1:n.*299C= | |
| ENST00000700437.1:c.1095C= | ENSP00000514988.1:p.Ala365= | |
| ENST00000700468.1:c.1233C= | ENSP00000515001.1:p.Ala411= | |
| ENST00000700469.1:c.1332C= | ENSP00000515002.1:p.Ala444= | |
| ENST00000324501.10:c.1344C= MANE Select | ENSP00000326366.5:p.Ala448= | |
| ENST00000324501.9:c.1344C= | ENSP00000326366.5:p.Ala448= | |
| ENST00000357710.8:c.1332C= | ENSP00000350342.4:p.Ala444= | |
| ENST00000394164.5:c.1332C= | ENSP00000377719.1:p.Ala444= | |
| ENST00000406768.1:c.1068C= | ENSP00000385948.1:p.Ala356= | |
| ENST00000555386.5:c.1424C= | ENSP00000450845.1:n.1424C= | |
| ENST00000555867.1:n.709C= | ||
| ENST00000557511.5:c.1170C= | ENSP00000451429.1:p.Ala390= | |
| NM_000021.3:c.1344C= | NP_000012.1:p.Ala448= | |
| NM_007318.2:c.1332C= | NP_015557.2:p.Ala444= | |
| XM_005267864.1:c.1344C= | XP_005267921.1:p.Ala448= | |
| XM_005267866.1:c.1332C= | XP_005267923.1:p.Ala444= | |
| XM_011536971.1:c.1344C= | XP_011535273.1:p.Ala448= | |
| XM_011536972.1:c.1344C= | XP_011535274.1:p.Ala448= | |
| XM_011536973.1:c.1332C= | XP_011535275.1:p.Ala444= | |
| XM_011536974.1:c.1332C= | XP_011535276.1:p.Ala444= | |
| XM_005267864.3:c.1344C= | XP_005267921.1:p.Ala448= | |
| XM_005267866.2:c.1332C= | XP_005267923.1:p.Ala444= | |
| XM_011536972.2:c.1344C= | XP_011535274.1:p.Ala448= | |
| XM_011536973.2:c.1332C= | XP_011535275.1:p.Ala444= | |
| XM_011536974.2:c.1332C= | XP_011535276.1:p.Ala444= | |
| NM_000021.4:c.1344C= MANE Select | NP_000012.1:p.Ala448= | |
| NM_007318.3:c.1332C= | NP_015557.2:p.Ala444= |